| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31729755-31729856 | Common:1; Rare:20 | ||||
| chr6:31730176-31730382 | Common:2; Rare:65 | ||||
| chr6:31736378-31736583 | Common:1; Rare:38 | ||||
| chr6:31815340-31815555 | Common:1; Rare:69 | ||||
| chr6:31827474-31827759 | Common:2; Rare:93 | ||||
| chr6:31897673-31897782 | Rare:20 | ||||
| chr6:31949305-31949532 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr6:31958892-31959195 | Rare:100; Clinvar:8 | ||||
| chr6:32117680-32117978 | Common:2; Rare:69 | ||||
| chr6:32127722-32127906 | Rare:49 | ||||
| chr6:32154376-32154492 | Rare:14 | ||||
| chr6:32176057-32176248 | Common:1; Rare:38 | ||||
| chr6:32178144-32178512 | Common:2; Rare:65 | ||||
| chr6:32190131-32190306 | Rare:37 | ||||
| chr6:32192509-32192742 | Rare:44 |